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2-IODO-5-NITROANISOLE, with the molecular formula C7H6INO3, is a nitro compound characterized by an anisole group with both a nitro and an iodo group attached to the benzene ring. This chemical compound serves as a versatile building block in the synthesis of a range of organic compounds, including pharmaceuticals, agrochemicals, and dyes. Additionally, it is utilized in research and chemical analysis, making it a significant component in various scientific and industrial applications. However, due to potential health and environmental hazards, it requires careful handling and adherence to proper safety measures.

5458-84-4

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5458-84-4 Usage

Uses

Used in Pharmaceutical Industry:
2-IODO-5-NITROANISOLE is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure allows for the creation of new drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-IODO-5-NITROANISOLE is used as a precursor in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Dye Industry:
2-IODO-5-NITROANISOLE is utilized as a building block in the production of dyes, enabling the creation of a variety of colorants for different applications, including textiles, plastics, and printing inks.
Used in Research and Chemical Analysis:
2-IODO-5-NITROANISOLE is employed as a research compound in various scientific studies, aiding in the understanding of chemical reactions and the development of new methodologies in chemical analysis.
Safety Precautions:
Due to the potential health and environmental hazards associated with 2-IODO-5-NITROANISOLE, it is crucial to handle 2-IODO-5-NITROANISOLE with caution. Proper safety measures, including the use of personal protective equipment, should be implemented to minimize risks during its synthesis, storage, and application.

Check Digit Verification of cas no

The CAS Registry Mumber 5458-84-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5458-84:
(6*5)+(5*4)+(4*5)+(3*8)+(2*8)+(1*4)=114
114 % 10 = 4
So 5458-84-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H6INO3/c1-12-7-4-5(9(10)11)2-3-6(7)8/h2-4H,1H3

5458-84-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodo-5-nitroanisole

1.2 Other means of identification

Product number -
Other names 1-iodo-2-methoxy-4-nitrobenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5458-84-4 SDS

5458-84-4Relevant academic research and scientific papers

2-Methoxy-4-nitrobenzenediazonium salt as a practical diazonium-transfer agent for primary arylamines via tautomerism of 1,3-diaryltriazenes: Deaminative iodination and arylation of arylamines without direct diazotization

Saeki, Tomoyuki,Son, Eun-Cheol,Tamao, Kohei

, p. 1654 - 1658 (2007/10/03)

1,3-Diaryltriazenes, prepared from a 2-methoxy-4-nitrobenzenediazonium salt and primary arylamines, exist as "azo-transfer" tautomers in which the 2-methoxy-4-nitrophenyl group is present on the saturated nitrogen atom and forms a hydrogen bond between the 2-methoxy group and the N-H moiety. The synthetic utility of the diazonium salt as a practical diazonium-transfer agent for primary arylamines via tautomerism of the 1,3-diaryltriazenes has been demonstrated by the deaminative iodination and arylation of the arylamines without direct diazotization. The starting 2-methoxy-4-nitrophenylamine can be easily recovered after the reactions.

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